@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP159676.RAlQY1hMI7Lv6Bl58UnjhxkNK20r86sBVGNY56G1S4hHE
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP159676.RAlQY1hMI7Lv6Bl58UnjhxkNK20r86sBVGNY56G1S4hHE130_head
{
this:
np:hasAssertion
dgn-np:NP159676.RAlQY1hMI7Lv6Bl58UnjhxkNK20r86sBVGNY56G1S4hHE130_assertion
;
np:hasProvenance
dgn-np:NP159676.RAlQY1hMI7Lv6Bl58UnjhxkNK20r86sBVGNY56G1S4hHE130_provenance
;
np:hasPublicationInfo
dgn-np:NP159676.RAlQY1hMI7Lv6Bl58UnjhxkNK20r86sBVGNY56G1S4hHE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP159676.RAlQY1hMI7Lv6Bl58UnjhxkNK20r86sBVGNY56G1S4hHE130_assertion
a
np:Assertion
.
dgn-np:NP159676.RAlQY1hMI7Lv6Bl58UnjhxkNK20r86sBVGNY56G1S4hHE130_provenance
a
np:Provenance
.
dgn-np:NP159676.RAlQY1hMI7Lv6Bl58UnjhxkNK20r86sBVGNY56G1S4hHE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP159676.RAlQY1hMI7Lv6Bl58UnjhxkNK20r86sBVGNY56G1S4hHE130_assertion
{
miriam-gene:49
a
ncit:C16612
.
lld:C0520463
a
ncit:C7057
.
dgn-gda:DGN87440387481661485fa03a73652f79f3
sio:SIO_000628
miriam-gene:49
,
lld:C0520463
;
a
sio:SIO_001121
.
}
dgn-np:NP159676.RAlQY1hMI7Lv6Bl58UnjhxkNK20r86sBVGNY56G1S4hHE130_provenance
{
dgn-np:NP159676.RAlQY1hMI7Lv6Bl58UnjhxkNK20r86sBVGNY56G1S4hHE130_assertion
dcterms:description
"[Mutation analysis of CYP21A2 gene was performed in seven patients with congenital adrenal hyperplasia (CAH) by combining differential long template polymerase chain reaction (PCR) amplification and amplified created restriction site (ACRS) methods.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:11431859
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP159676.RAlQY1hMI7Lv6Bl58UnjhxkNK20r86sBVGNY56G1S4hHE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:26+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}